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Author: Jaana Suvisaari

  • Most recently observed institution: National Institute for Health and Welfare, Helsinki, Finland

Rankings

  • All-time downloads: 8,399 (rank: 6,319 out of 310,086)
  • Categories:
    • genetics: 5,749 (rank: 2,651 out of 30,681)
    • genomics: 2,650 (rank: 5,836 out of 34,981)

Downloads per author, site-wide

Preprints

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

genetics more details view paper
  • Downloaded 2,207 times
  • Download rankings, all-time:
    • Site-wide: 2,183 out of 71,071
    • In genetics: 201 out of 3,937
  • Year to date:
    • Site-wide: 37,780 out of 71,071
  • Since beginning of last month:
    • Site-wide: 61,723 out of 71,071

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
  • Downloaded 1,628 times
  • Download rankings, all-time:
    • Site-wide: 3,682 out of 71,071
    • In genetics: 311 out of 3,937
  • Year to date:
    • Site-wide: 40,692 out of 71,071
  • Since beginning of last month:
    • Site-wide: 39,330 out of 71,071

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,322 times
  • Download rankings, all-time:
    • Site-wide: 5,239 out of 71,071
    • In genomics: 908 out of 4,740
  • Year to date:
    • Site-wide: 46,677 out of 71,071
  • Since beginning of last month:
    • Site-wide: 22,909 out of 71,071

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 929 times
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    • In genomics: 1,420 out of 4,740
  • Year to date:
    • Site-wide: 36,015 out of 71,071
  • Since beginning of last month:
    • Site-wide: 49,560 out of 71,071

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 844 times
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    • Site-wide: 10,953 out of 71,071
    • In genetics: 796 out of 3,937
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  • Since beginning of last month:
    • Site-wide: 56,576 out of 71,071

Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

genetics more details view paper
  • Downloaded 494 times
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    • In genetics: 1,534 out of 3,937
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  • Since beginning of last month:
    • Site-wide: 33,630 out of 71,071

Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

genomics more details view paper
  • Downloaded 399 times
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    • In genomics: 3,011 out of 4,740
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    • Site-wide: 17,460 out of 71,071
  • Since beginning of last month:
    • Site-wide: 39,576 out of 71,071

The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to MicroRNA-484

genetics more details view paper
  • Downloaded 321 times
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    • Site-wide: 36,957 out of 71,071
    • In genetics: 2,270 out of 3,937
  • Year to date:
    • Site-wide: 39,786 out of 71,071
  • Since beginning of last month:
    • Site-wide: 59,812 out of 71,071

Variants in regulatory elements of PDE4D associate with Major Mental Illness in the Finnish population

genetics more details view paper
  • Downloaded 255 times
  • Download rankings, all-time:
    • Site-wide: 44,562 out of 71,071
    • In genetics: 2,678 out of 3,937
  • Year to date:
    • Site-wide: 40,292 out of 71,071
  • Since beginning of last month:
    • Site-wide: 56,302 out of 71,071

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